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. 2004 Apr;186(7):2147–2155. doi: 10.1128/JB.186.7.2147-2155.2004

TABLE 6.

cydA sequence changes observed in suppressor isolatesa

Suppressor isolate Cotransduction frequency Base change Base position Amino acid position Amino acid change
PS1 0
PS3 0.89 C→T 770934 85 Ser→Phe
1A None
1B 0.96 G→A 771129 150 Trp→stop
1C 0.83 None
1D 0.79 C→T 770934 85 Ser→Phe
1E 0.75 None
1F G→A 771295 205 Trp→stop
1G 0.91 None
1H 0.85 None
1I 0.79 C→T 771003 108 Ser→Phe
1K 0.83
1L G→A 771392 238 Gly→Ser
1M 0.88 None
1Nb 0.79 C→T 771402 241 Ser→Phe
1Nb C→T 771477 266 Pro→Leu
1O 0.79 None
1P 0.96 None
1Q 0.95 None
1R 0.78 G→T 770888 70 Gly→Cys
1S 0.87 C→T 771668 330 Gln→stop
1Z 0.85 G→A 771460 261 Trp→stop
2A 0.84 G→A 771460 261 Trp→stop
2B 0 None
2E 0.85 None
2F 0.94 G→A 771395 240 Asp→Asn
2J 0.79 G→A 771392 239 Gly→Ser
2K 0.8 None
2N 0.93 G→A 770922 82 Trp→stop
2Q 0.65 G→A 771788 371 Ala→Thr
a

Sequences were determined for the cydA gene from E. coli nucleotides 770738 to 772249 by using PCR products and primers described in Table 2 and sequencing in both directions. The cydA gene runs from nucleotide 770678 to nucleotide 772249. The cotransduction frequency is the fraction of replacements of cydA by cydA+ in a cross with phage P1 grown on a cydA+ nadA57::Tn10 strain. Frequencies were determined from 96 isolates screened as described in Materials and Methods. The nucleotide positions are the positions in the sequence published by Blattner et al. (6). The amino acid positions are the positions in the protein rather than the positions calculated from the gene sequence since the first ATG does not appear in the protein.

b

Two base changes were found in the cydA region of this isolate.